A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516391



Internal ID20889752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37610883..37611720hg38UCSC Ensembl
chr18:35190846..35191683hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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